7292-71-9 Usage
Description
AMINO-(3-CHLORO-PHENYL)-ACETIC ACID is an organic compound that serves as an intermediate in the synthesis of various pharmaceuticals and is utilized in the structure-activity relationship examination of drugs containing the benzyl moiety. Its unique chemical structure allows it to play a significant role in the development and understanding of drugs involved in biochemical and pharmacological processes.
Uses
Used in Pharmaceutical Industry:
AMINO-(3-CHLORO-PHENYL)-ACETIC ACID is used as an intermediate in the preparation of synthetic penicillins, which are a class of antibiotics essential for treating a wide range of bacterial infections.
Used in Drug Development Research:
AMINO-(3-CHLORO-PHENYL)-ACETIC ACID is used in the structure-activity relationship examination of several drugs containing the benzyl moiety. This helps researchers understand the relationship between the chemical structure of these drugs and their biological activity, ultimately leading to the development of more effective and safer medications.
Used in Biochemical and Pharmacological Processes:
AMINO-(3-CHLORO-PHENYL)-ACETIC ACID plays a role in understanding the mechanisms of action of various drugs and their interactions with biological systems. This knowledge is crucial for the advancement of drug discovery and the improvement of existing therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 7292-71-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,9 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7292-71:
(6*7)+(5*2)+(4*9)+(3*2)+(2*7)+(1*1)=109
109 % 10 = 9
So 7292-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H8ClNO2/c9-6-3-1-2-5(4-6)7(10)8(11)12/h1-4,7H,10H2,(H,11,12)
7292-71-9Relevant articles and documents
Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine
Inada, Haruki,Shibuya, Masatoshi,Yamamoto, Yoshihiko
, p. 11047 - 11059 (2020/10/12)
The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate the use of commercially available l-2-(2-chlorophenyl)glycine as the nitrogen source in the transamination of arylglyoxylic acids, producing the corresponding 2-arylglycines without interference from the undesired self-transamination process.
PLATELET ADP RECEPTOR INHIBITORS
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Page/Page column 55, (2008/06/13)
Compounds are provided which are useful as platelet ADP receptor inhibitors, for treating thrombosis and for reducing the likelihood and/or severity of a secondary ischemic event in a patient.
Synthesis of some chlorosubstituted DL-phenylamino acid alkylester hydrochlorides
Kobow,Sprung,Schulz
, p. 529 - 530 (2007/10/02)
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